Fatal drug reaction to andexanet alfa: a case report

EJHaem Pub Date : 2024-06-22 DOI:10.1002/jha2.959
Richard J. Buka, Mamidipudi T. Krishna, David J. Sutton
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Abstract

Andexanet alfa is a recombinant, modified factor Xa (FXa) molecule that is used for the reversal of the anticoagulant effect of oral anti-FXa anticoagulants in patients with major haemorrhage. Here, we present a case of an 85-year-old man taking rivaroxaban for atrial fibrillation, who presented with an acute, upper gastrointestinal bleed. He was stabilised with red cell transfusion and then received a 400 mg bolus of andexanet alfa. Within minutes of this, he developed chest tightness, shortness of breath, ischaemic electrocardiographic changes and then cardiac arrest from which he could not be resuscitated. The onset of symptoms was clearly temporally related to andexanet alfa administration and the differential diagnosis includes anaphylaxis with Kounis syndrome, or myocardial infarction. Although infusion site reactions have been reported and are relatively common, this is to date the first case of a fatal drug reaction andexanet alfa. This knowledge can be factored into physicians’ risk–benefit decisions when treating patients with oral anti-FXa anticoagulant-associated major haemorrhage.

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对安赛蜜α的致命药物反应:一份病例报告
Andexanet alfa 是一种重组的改良 Xa 因子 (FXa) 分子,用于逆转大出血患者口服抗 FXa 抗凝剂的抗凝作用。在此,我们介绍了一例因心房颤动服用利伐沙班的 85 岁老人的病例,他出现了急性上消化道出血。他在输注红细胞后病情稳定,随后接受了 400 毫克的安赛蜜α栓剂。几分钟后,他出现胸闷、气短、缺血性心电图改变,随后心跳骤停,抢救无效死亡。症状的出现显然与服用安克沙奈α有关,鉴别诊断包括过敏性休克伴库尼斯综合征或心肌梗死。虽然输液部位反应已有报道且相对常见,但这是迄今为止首例致死性药物反应 andexanet alfa。医生在治疗与口服抗 FXa 抗凝剂相关的大出血患者时,可将这一知识纳入风险效益决策中。
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